Safety and efficacy of a Vero-adapted live attenuated vaccine candidate for African swine fever

IF 4.5 3区 医学 Q2 IMMUNOLOGY Vaccine Pub Date : 2025-05-22 Epub Date: 2025-04-24 DOI:10.1016/j.vaccine.2025.127172
Tae-Young Suh , Ji-Hoon Park , Seong Yun Hwang , Chae-Rin Park , Ji-Eun Kim , Jun Young Park , Yong-Joo Kim , Hae-Eun Kang , Dae-Yong Kim , Jun-Gu Choi
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Abstract

African swine fever (ASF) is a lethal disease that significantly affects the global swine industry owing to the high mortality rate of infected pigs. The causative agent, ASF virus (ASFV), is difficult to control; however, live attenuated vaccines have recently emerged as a promising solution. This study evaluated the safety and efficacy of a novel live attenuated ASFV strain (VaCln3 P13) derived from a Korean ASFV isolate adapted to Vero cells. VaCln3 P13 harbors 12 non-synonymous SNPs across multiple viral genes without large gene deletions, all of which may collectively contribute to its attenuated phenotype. Notably, mutations in MGF300-2R and MGF505-7R result in protein truncation potentially influencing its safety. Our evaluation in domestic pigs inoculated with varying doses of VaCln3 P13, demonstrated substantial attenuation and protective efficacy against a virulent ASFV challenge, with only transient clinical signs and no severe adverse effects. All vaccinated pigs developed robust humoral immune responses and overcame the virulent parental virus challenge and survived, whereas mock-inoculated pigs succumbed within 10 days post-challenge. Pathological assessments revealed limited histopathological lesions in vaccinated pigs, while unvaccinated controls displayed extensive hemorrhage, lymphoid depletion, and severe systemic lesions after the challenge. These findings underscore the potential of VaCln3 P13 as a vaccine candidate for ASF control and hold promise for further applications.
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一种适应vero的非洲猪瘟候选减毒活疫苗的安全性和有效性
非洲猪瘟(ASF)是一种致命疾病,由于感染猪的高死亡率,严重影响全球养猪业。病原体非洲猪瘟病毒(ASFV)难以控制;然而,减毒活疫苗最近成为一种有希望的解决方案。本研究评估了一种新型ASFV减毒活毒株(VaCln3 P13)的安全性和有效性,该毒株来源于适应于Vero细胞的韩国ASFV分离株。VaCln3 P13包含12个跨多个病毒基因的非同义snp,没有大的基因缺失,所有这些可能共同导致其表型减弱。值得注意的是,MGF300-2R和MGF505-7R突变导致蛋白质截断,可能影响其安全性。我们在接种不同剂量VaCln3 P13的家猪中进行的评估显示,对ASFV的致命攻击有明显的衰减和保护作用,只有短暂的临床症状,没有严重的不良反应。所有接种过疫苗的猪都产生了强大的体液免疫反应,克服了毒母病毒的攻击并存活下来,而模拟接种的猪在攻击后10天内死亡。病理评估显示,接种疫苗的猪有有限的组织病理学病变,而未接种疫苗的对照组在攻击后表现出广泛的出血、淋巴细胞耗竭和严重的全身病变。这些发现强调了vacln3p13作为控制非洲猪瘟候选疫苗的潜力,并有望进一步应用。
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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